Below you will see a wedge-dash diagram, and an incomplete Newman projection with the designated bond you are looking down. Your task is to complete the Newman projection, by filling-in each box below, with the substituents (e.g. CH3, Br, H, etc.- whichever substituents remain in the molecule) that would give the MOST STABLE conformer.

Below you will see a wedge-dash diagram, and an incomplete Newman projection with the designated bond you are looking down. Your task is to complete the Newman projection, by filling-in each box below, with the substituents (e.g. CH3, Br, H, etc.- whichever substituents remain in the molecule) that would give the MOST STABLE conformer.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

See similar textbooks

Similar questions

2. Which of the following Newman projections shows the most stable conformation of a molecule? (Circle one.) Меме Et Ме Ме Н. Et Ме Ме iPr Me- H. Me Me Me Me Me `Et H H H A В D 3. Select the Newman projection of the following compound as viewed down the bond indicated. (Circle one.) Ме 'Bu iPr Me Me Ме. Ме Me H "Ме H. H H. Me Me Ме А В C
3. Looking at the structure of the compound below (2,2-dimethylbutane), sighting down the C2-C3 bond) draw a Newman project for the most stable configuration. H3C CH3 H3C CH3
Is my answer correct? Not too sure.
Given cyclohexane in a chair conformation, construct the more stable conformation of cis-1-ethyl-2-fluorocyclohexane by filling in the missing atoms or groups. Use the numbering provided on the ring. 1 H T Answer Bank H 5 6 H ethyl H H 4 3 T H H
Create a conformational analysis using the molecule in the picture. Follow the instruction in the picture when you transform the molecule into its Newman projection. Explain the conformations.
draw most stable and least stable conformations for each
Create a conformational analysis using the molecule in the picture. Follow the instruction in the picture when you transform the molecule into its Newman projection. Which conformer is the most unstable? Explain.
Organic Chem HW
Using solid and dashed wedges, draw the structure of (1S, 2S, 4R, 5R)-1,5-dibromo-2,4- dichlorocyclohexane, then draw the most stable conformer.
Starting from the structure below (sighting down the indicated bond). rotate the back carbon to provide an eclipsed conformer of the structure. Ph H H HI!!! ++||||4 CH₂CH3 I I I I I I H Draw Newman Projection I I I
6. Sort the following conformations of 1-chloropropane from most stable to least stable. H CI Hн Н Н Н CH₂ н H н CI 2) Н CH, H 3) CH1 CI
2) a) Provide Newman projects of the three staggered conformations of molecule 1 shown below looking down the indicated bond (1→2). Circle the most stable conformation. HH3C CH3 H molecule 1 b) Provide Newman projects of the three eclipsed conformations of molecule 1 looking down the indicated bond. Put a square around the least stable conformation.